Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mutations at arginine residues in two Asian hemophilia B patients.

Nucleic acids research - 11 Apr 1990

Bottema C D, Ketterling R P, Koeberl D D, Taylor S A, Sommer S S

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Arginine
Share to Asia
Share to Codon
Share to Factor X

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hemophilia A

Share to Mutation

Share to Polymorphism, Restriction Fragment Length

Source

Open in PubMed Open full text

Identifiers

PMID: 1970868
DOI: 10.1093/nar/18.7.1924
PMCID: PMC330647

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutations at arginine residues in two Asian hemophilia B patients.PMID 1970868Read ↗

Mutations associated with hemophilia B in Turkish patients.Semantic proximity Read ↗

Three missense mutations in Arg codons of the factor VIII genes of mild to moderately severe hemophilia A patients.Semantic proximity Read ↗

Amino acid substitutions in the factor VIII coagulation protein that cause hemophilia A in man.Semantic proximity Read ↗

An amino acid contributing to pockets A, B, and D of the peptide-binding groove is altered in A*0315.Semantic proximity Read ↗

A novel point mutation in severe haemophilia A: a further proof of genotype-phenotype correlation.Semantic proximity Read ↗

Recurrent nonsense mutations at arginine residues cause severe hemophilia B in unrelated hemophiliacs.Semantic proximity Read ↗

A novel A allele with c.467C > T and c.784G > A nucleotide substitutions in Korean individuals.Semantic proximity Read ↗

Amino acid substitutions in conserved domains of factor VIII and related proteins: study of patients with mild and moderately severe hemophilia A.Semantic proximity Read ↗

Identification of six novel F9 mutations among haemophilia B patients from Macedonia and Bulgaria.Semantic proximity Read ↗

A novel nucleotide deletion in RHAG allele identified in a Chinese Rhnull individual.Semantic proximity Read ↗

F9 mutations causing deletions beyond the serine protease domain confer higher risk for inhibitor development in hemophilia B.Semantic proximity Read ↗

Haemophilia B: database of point mutations and short additions and deletions--second edition.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.